ISO/IEC 17025:2017(E)
c) determination of the performance characteristics of the method;
d) results obtained;
e) a statement on the validity of the method, detailing its fitness for the intended use.
7.3 Sampling
7.3.1 The laboratory shall have a sampling plan and method when it carries out sampling of substances,
materials or products for subsequent testing or calibration. The sampling method shall address the
factors to be controlled to ensure the validity of subsequent testing or calibration results. The sampling
plan and method shall be available at the site where sampling is undertaken. Sampling plans shall,
whenever reasonable, be based on appropriate statistical methods.
7.3.2 The sampling method shall describe:
a) the selection of samples or sites;
b) the sampling plan;
c) the preparation and treatment of sample(s) from a substance, material or product to yield the
required item for subsequent testing or calibration.
NOTE
When
received into the laboratory, further handling can be required as specified in
7.4
.
7.3.3 The laboratory shall retain records of sampling data that forms part of the testing or calibration
that is undertaken. These records shall include, where relevant:
a) reference to the sampling method used;
b) date and time of sampling;
c) data to identify and describe the sample (e.g. number, amount, name);
d) identification of the personnel performing sampling;
e) identification of the equipment used;
f) environmental or transport conditions;
g) diagrams or other equivalent means to identify the sampling location, when appropriate;
h) deviations, additions to or exclusions from the sampling method and sampling plan.
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